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1 ith CNQX, AP-5, strychnine, bicuculline, and carbenoxolone.
2 0 or 1750 mg/kg diet), or DHEA + tamoxifen + carbenoxolone.
3  were blocked by the Cx43 blockers Gap26 and carbenoxolone.
4 ion was blocked by the 11beta-HSD2 inhibitor carbenoxolone.
5 as impaired in the presence of probenecid or carbenoxolone.
6 e inhibitors Brilliant Blue, gadolinium, and carbenoxolone.
7 llular loops abrogates channel inhibition by carbenoxolone.
8 harmacological uncoupling with 20-micromol/L carbenoxolone.
9 osphate release inhibitors glibenclamide and carbenoxolone.
10 eurons via a mechanism that was sensitive to carbenoxolone.
11 s was attenuated by the gap junction blocker carbenoxolone.
12 ing was reversibly blocked by application of carbenoxolone.
13 h were sensitive to the gap junction blocker carbenoxolone.
14 d by the gap junction blockers 1-octanol and carbenoxolone.
15  were attenuated by the gap junction blocker carbenoxolone.
16 y by the gap junction inhibitors octanol and carbenoxolone.
17         Octanol (260.46 mg or 781.38 mg/kg), carbenoxolone (100 mg/kg), or vehicles were given via in
18       The non-specific gap junction blockers carbenoxolone (100 microM) and octanol (1 mM) attenuated
19         However, the gap junction inhibitors carbenoxolone (100 microM) and palmitoleic acid (50 micr
20                    The gap junction blockers carbenoxolone (100 microm) or octanol (1 mM) significant
21 connexin channel blockers octanol (1 mm) and carbenoxolone (100 mum).
22 elial denudation or gap junction inhibition (carbenoxolone; 100 um) increased SMC death, inhibiting N
23          Gap junction uncouplers (1-octanol, carbenoxolone, 18beta-glycyrrhetinic acid and connexin m
24                                  Addition of carbenoxolone (200 microM), a gap junction channel block
25  to morphine was significantly attenuated by carbenoxolone (25 mg/kg).
26         Partial gap junction uncoupling with carbenoxolone (25 mumol/L) increased focal activity (2.1
27 moxifen (80 or 40 microgram/kg diet), DHEA + carbenoxolone (3500 or 1750 mg/kg diet), or DHEA + tamox
28                                 In addition, carbenoxolone (a gap junction blocker) decreased the cum
29            Spinal (intrathecal) injection of carbenoxolone (a non-selective hemichannel blocker) and
30                                  The IC50 of carbenoxolone, a competitive inhibitor of 11beta-HSD, wa
31                                              Carbenoxolone, a Cx43 gap junction uncoupler, markedly p
32 re obtained from crus 2a Purkinje cells, and carbenoxolone, a gap junction blocker, was injected into
33 mitter receptor antagonists and disrupted by carbenoxolone, a gap junction blocker.
34                                              Carbenoxolone, a gap junction inhibitor, antagonized mod
35                                  Addition of carbenoxolone, a PANX1 channel blocker, completely aboli
36 normal IO neurons, a finding replicated with carbenoxolone, a pharmacological antagonist of gap junct
37                                              Carbenoxolone abolished all synchronized IPSPs in CA3 ce
38                   The gap junction inhibitor carbenoxolone abolished both electrical and tracer coupl
39 rgic currents, we tested the hypothesis that carbenoxolone acted via specific sites on GABAA receptor
40 lutamate and ATP flux and that the inhibitor carbenoxolone acts from the extracellular side, binding
41                              Neither THA nor carbenoxolone affected electrically stimulated action po
42                                              Carbenoxolone also blocked the isolated synchronized GAB
43                                              Carbenoxolone also depressed responses to exogenous and
44             Likewise, gap junction inhibitor carbenoxolone also inhibited self-assembly of KGN, NHF,
45                       When further examined, Carbenoxolone also led to a significant reduction in inf
46                                              Carbenoxolone also prevented gut wall disruption and sig
47 5, and functional blockade of connexins with carbenoxolone also prevented the in vitro formation of f
48                                              Carbenoxolone also reduced the average firing rate by 50
49 hagocytosis by Hsd11b1(-/-) macrophages, and carbenoxolone, an 11beta-HSD inhibitor, prevented the in
50 exus of the mouse colon; the Cx43 inhibitors carbenoxolone and 43Gap26 inhibited the ability of enter
51        Conversely, the gap junction blockers carbenoxolone and cobalt decreased neuronal CO2/H+ sensi
52                                 By contrast, carbenoxolone and cobalt reduced bright surround, sugges
53                                              Carbenoxolone and cobalt, thought to attenuate feedback
54 e phase, and this increase was suppressed by carbenoxolone and Gap27, and recapitulated by CXCL1.
55 lease was abolished by the channel inhibitor carbenoxolone and inhibited by knockdown of either conne
56            The glycynhetinic acid derivative carbenoxolone and intracellular acidification with CO2 d
57 e in the presence of the pannexin 1 blockers carbenoxolone and probenecid, and the HlyA-induced ATP r
58                               Treatment with carbenoxolone and probenecid, which directly and specifi
59 nc, or AZ 10606120, and by pannexin blockers carbenoxolone and probenecid.
60 us ATP can reverse the inhibitive effects of carbenoxolone and that aggregate compaction is sensitive
61    Cell-to-cell propagation was abolished by carbenoxolone, and was not observed in uncoupled pairs.
62 d that the observed antiepileptic effects of carbenoxolone are likely to be due to blockade of GABAA
63 in the extracellular entrance and a role for carbenoxolone as a channel blocker.
64                              We identified a carbenoxolone-binding site embraced by W74 in the extrac
65            The administration of octanol and carbenoxolone both failed to attenuate the neurological
66 n apo state, a caspase-7-cleaved state and a carbenoxolone-bound state.
67 1 hemichannels with (10)Panx, probenecid, or carbenoxolone but not when connexin hemichannels were in
68                                    Moreover, carbenoxolone caused a reduction in the approximately 10
69 -dione (CNQX) and the gap-junction blockers, carbenoxolone (CBX) and meclofenamic acid (MEC).
70 ats, inhibition of pannexin 1 channels using carbenoxolone (CBX) or Brilliant Blue FCF (BB-FCF) (1-10
71                               VRAC blockade (carbenoxolone, CBX, 100 muM, 20 min) enhanced dilation o
72 ely, in CTL hearts, gap junction inhibition (carbenoxolone) decreased coupling and allowed Ca wave-in
73 lockade of gap junctional communication with carbenoxolone did not induce neuronal differentiation in
74                        Hemichannel inhibitor carbenoxolone disodium and the exocytotic pathway of tra
75 ly administration of a gap junction blocker, carbenoxolone, during the first postnatal week greatly d
76 l inhibitors 18 beta-glycyrrhetinic acid and carbenoxolone, even in cells without physical contact, s
77 ficity of gap junction blockers (18-beta-GA, carbenoxolone, flufenamic acid and heptanol) in paired r
78 unction channel blockers (heptanol, octanol, carbenoxolone, flufenamic acid, and mefloquine) are anta
79 vity in three different coupling conditions: carbenoxolone (gap junctions blocker), control, and picr
80 mokine CXCL1, and the release was blocked by carbenoxolone, Gap26/Gap27, and connexin-43 small interf
81                                              Carbenoxolone (IC50 = 2 microM) and 4-methylpyrazole (IC
82 ed cognition, and the nonselective inhibitor carbenoxolone improved verbal memory in elderly men.
83 ft ventricle, left atrium, and right atrium, carbenoxolone increased R(j) by 28+/-9%, 26+/-16%, and 2
84                   The gap junction inhibitor carbenoxolone increases the spontaneous activity of supr
85                      Inhibitor studies using carbenoxolone indicated that blocking innexons resulted
86 icantly affected by the gap junction blocker carbenoxolone, indicating that outward events originated
87 Three independent inhibitors of hemichannels-carbenoxolone, lanthanum and mefloquine-had no significa
88 d La3+) and by gap junction blocking agents (carbenoxolone, octanol, heptanol, flufenamic acid, and 1
89  Reduction in gap junction conductance using carbenoxolone only minimally affected APD distribution i
90      Moreover, cell death was prevented with carbenoxolone or (10)Panx1 in Delta371hPanx1 cells, wher
91 ducing gap junctional conductance (Gj) using carbenoxolone or by backcrossing into a cardiomyocyte-sp
92 turbing outer retinal signalling with either carbenoxolone or cobalt blocked the effects of the brigh
93 eliminated by blocking synaptic ATP release (carbenoxolone) or degrading extracellular ATP (apyrase).
94  A740003) and Px1 HC blockers ((10)Panx1 and carbenoxolone) prevent the increase in Etd(+) uptake by
95                       Release was blocked by carbenoxolone, probenecid or peptide (10)panx, implicati
96 frequency component of 75.5 +/- 5.6 %, while carbenoxolone produced a reduction of only 14 +/- 42 %.
97 n slowing in vivo in the intact human heart, carbenoxolone prolonged electrogram duration in the righ
98 man and guinea-pig myocardium, pre- and post-carbenoxolone (r(2)=0.946; P<0.01).
99                                              Carbenoxolone reduced CS synchrony by 50% overall, but i
100 drenal gap junctions by the uncoupling agent carbenoxolone reduces nerve stimulation-evoked catechola
101                   Pharmacological testing of Carbenoxolone-related compounds, acting by inhibition of
102 but just a few of these compounds, including Carbenoxolone, remained active when tested in a post-tre
103 nel inhibitors octanol, flufenamic acid, and carbenoxolone significantly blocked spontaneous activity
104 xin/gap junction channels with probenecid or carbenoxolone significantly reduced external dentin stim
105 Population activity was greatly depressed by carbenoxolone, suggesting that propagation of depolarizi
106 ly isolated optic nerve) that was blocked by carbenoxolone, suggesting the existence of functional he
107         Blockade of electrical coupling with carbenoxolone suppressed amplitude, frequency and half-w
108 he connexin 43 (Cx43) mimetic peptide Gap26, carbenoxolone, the pannexin1 (Panx1) mimetic peptide (10
109 suppression was inhibited by the addition of carbenoxolone to cocultures, suggesting that gap junctio
110             We used the gap junction blocker carbenoxolone to investigate the role of electrotonic co
111 al administration of the 11betaHSD inhibitor carbenoxolone to uremic rats for 2 wk improved glucose t
112 blished gap junction inhibitors: octonal and carbenoxolone, to interrupt cell to cell communication w
113 s accompanied by a decline in TEP1 levels in carbenoxolone-treated mosquitoes.
114                                      Lastly, carbenoxolone was found to reverse or prevent changes in
115                                              Carbenoxolone washout restored activity.
116  and sensitive to the gap junction inhibitor carbenoxolone, whereas the effect on electrical activity
117 f 18beta-glycyrrhetinic acid (18beta-GA) and carbenoxolone, which have been shown to block electrical

 
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